|Publication number||US7499759 B2|
|Application number||US 10/972,298|
|Publication date||Mar 3, 2009|
|Filing date||Oct 22, 2004|
|Priority date||Oct 24, 2003|
|Also published as||US20050137674|
|Publication number||10972298, 972298, US 7499759 B2, US 7499759B2, US-B2-7499759, US7499759 B2, US7499759B2|
|Inventors||M. Sean Coe, Ronald W. Heil, Jr., Peter T. Kelley, Jason Alan Shiroff, Randy W. Westlund, F. Palme II Donald|
|Original Assignee||Cardiac Pacemakers, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (86), Non-Patent Citations (17), Referenced by (1), Classifications (7), Legal Events (4)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present application claims the benefit of the following U.S. Provisional Applications: Application Ser. No. 60/514,037 filed Oct. 24, 2003, entitled “Absorbable Myocardial Lead Fixation System”, Application Ser. No. 60/514,665 filed Oct. 27, 2003, entitled “Lead Electrode Arrangement for Myocardial Leads”, Application Ser. No. 60/514,042 filed Oct. 24, 2003, entitled “Tapered Tip for Myocardial Lead”, Application Ser. No. 60/514,714 filed Oct. 27, 2003, entitled “Minimally-Invasive Fixation Systems for Over-the-Tether Myocardial Leads”, Application Ser. No. 60/514,039 filed Oct. 24, 2003, entitled “Distal or Proximal Fixation of Over-the-Suture Myocardial Leads”, Application Ser. No. 60/514,146 filed Oct. 24, 2003, entitled “Myocardial Lead with Fixation Mechanism”, Application Ser. No. 60/514,038 filed Oct. 24, 2003, entitled “Delivery Instrument for Myocardial Lead Placement” and Application Ser. No. 60/514,713 filed Oct. 27, 2003, entitled “Drug-Eluting Myocardial Leads”, all of which are incorporated herein by reference.
Reference is hereby made to commonly assigned U.S. patent application Ser. No. 10/821,421, filed Apr. 9, 2004 entitled “Cardiac Electrode Anchoring System” and the following commonly assigned U.S. patent applications filed on an even date herewith, all of which are incorporated herein by reference: application Ser. No. 10/972,049, entitled “Myocardial Lead,” application Ser. No. 10/971,549, entitled “Myocardial Lead with Fixation Mechanism,” application Ser. No. 10/971,551, entitled “Myocardial Lead Attachment System” and application Ser. No. 10/971,577, entitled “Absorbable Myocardial Lead Fixation System.”
The present invention, as defined by the claims herein, was made by parties to a Joint Research Agreement between Cardiac Pacemakers, Inc. and Dr. Osypka, GmbH.
This invention relates generally to implantable lead assemblies for stimulating and/or sensing electrical signals in muscle tissue. More particularly, it relates to myocardially-implanted leads for cardiac stimulation.
Cardiac rhythm management systems are used to treat heart arrhythmias. Pacemaker systems are commonly implanted in patients to treat bradycardia (i.e., abnormally slow heart rate). A pacemaker system includes an implantable pulse generator and leads, which form the electrical connection between the implantable pulse generator and the heart. An implantable cardioverter defibrillator (“ICD”) is used to treat tachycardia (i.e., abnormally rapid heart rate). An ICD also includes a pulse generator and leads that deliver electrical energy to the heart.
The leads coupling the pulse generator to the cardiac muscle are commonly used for delivering an electrical pulse to the cardiac muscle, for sensing electrical signals produced in the cardiac muscle, or for both delivering and sensing. The leads are susceptible to categorization according to the type of connection they form with the heart. An endocardial lead includes at least one electrode at or near its distal tip adapted to contact the endocardium (i.e., the tissue lining the inside of the heart). An epicardial lead includes at least one electrode at or near its distal tip adapted to contact the epicardium (i.e., the tissue lining the outside of the heart). Finally, a myocardial lead includes at least one electrode at or near its distal tip inserted into the heart muscle or myocardium (i.e., the muscle sandwiched between the endocardium and epicardium). Some leads have multiple spaced apart distal electrodes at differing polarities and are known as bipolar type leads. The spacing between the electrodes can affect lead performance and the quality of the electrical signal delivered or sensed through the heart tissue.
The lead typically includes a flexible conductor surrounded by an insulating tube or sheath that extends from the electrode at the distal end to a connector pin at the proximal end. Endocardial leads are typically delivered transvenously to the right atrium or ventricle and commonly employ tines at a distal end for engaging the trabeculae.
The treatment of congestive heart failure (“CHF”), however, often requires left ventricular stimulation either alone or in conjunction with right ventricular stimulation. For example, cardiac resynchronization therapy (“CRT”) (also commonly referred to as biventricular pacing) is an emerging treatment for heart failure, which requires stimulation of both the right and the left ventricle to increase cardiac output. Left ventricular stimulation requires placement of a lead in or on the left ventricle near the apex of the heart. One technique for left ventricular lead placement is to expose the heart by way of a thoracotomy. The lead is then positioned so that one or more electrodes contact the epicardium or are embedded in the myocardium. Another method is to advance an epicardial lead endovenously into the coronary sinus and then advance the lead through a lateral vein of the left ventricle. The electrodes are positioned to contact the epicardial surface of the left ventricle.
The left ventricle beats forcefully as it pumps oxygenated blood throughout the body. Repetitive beating of the heart, in combination with patient movement, can sometimes dislodge the lead from the myocardium. The electrodes may lose contact with the heart muscle, or spacing between electrodes may alter over time.
There is a need for an improved myocardial pacing lead suitable for chronic implantation and an attachment system for stabilizing such a lead in the heart.
According to one embodiment, the present invention is a myocardial lead attachment system for securing a lead within the myocardium. The attachment system includes an anchor configured to engage the heart, a tether coupled to the anchor and a lead body. The lead body has a proximal end, a distal end, a lumen for accepting the tether and a lock housing in the lumen. A lock structure is on the tether and mates with the lock housing and restrains motion of the lead with respect to the tether in either of a proximal or a distal direction.
According to another embodiment, the present invention is a myocardial lead attachment system for securing a lead within the myocardium. The attachment system includes an anchor configured to engage the heart, a tether coupled to the anchor and a lead body. The lead body has a proximal end, a distal end and a lumen for accepting the tether. The attachment system further includes a distal lock for engaging the tether to the distal end of the lead body. The distal lock includes a lock structure formed on a distal end of the tether and a lock housing in the lumen. The lock structure mates with the lock housing and restrains motion of the lead body with respect to the tether in either of a proximal or a distal direction. The attachment system further includes a proximal lock for engaging the tether to the lead body proximal to the distal lock. The proximal lock includes a through-hole extending from the lumen through the lead body at a location the same as or proximal to the lock housing for receiving a portion of the tether proximal to the distal lock and a second lock structure on the tether coupling the tether to the lead body adjacent the through-hole.
According to another embodiment, the present invention is a myocardial lead attachment system for securing a lead within the myocardium. The attachment system includes an anchor configured to engage the heart, a tether coupled to the anchor and a lead body. The lead body has a proximal end, a distal end and a lumen for accepting the tether. The attachment system further includes a distal lock for engaging the tether to the distal end of the lead body. The distal lock includes a lock structure formed on a distal end of the tether and a lock housing in the lumen. The lock structure mates with the lock housing and restrains motion of the lead body with respect to the tether in either of a proximal or a distal direction. The attachment system further includes a proximal lock formed on the tether and adapted to mate with the proximal end of the lead body. The proximal lock includes a second lock structure formed on the tether for fixing the tether in frictional engagement to the proximal end of the lead body.
According to another embodiment, the present invention is a method of securing a myocardial lead in the myocardium. An anchor coupled to a distal end of a tether is advanced through the myocardium to an implant location. A myocardial lead is threaded onto the tether. The lead is advanced over the tether to the implant location. A distal end of the lead is locked onto the distal end of the tether at a first attachment site. The tether is tensioned and the tether is secured to the lead at a second attachment site proximal to the first attachment site.
This summary is not intended to describe each embodiment or every implementation of the present invention. Advantages and a more complete understanding of the invention will become apparent upon review of the detailed description and claims in conjunction with the accompanying drawings.
While the invention is amenable to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and are described in detail below. The intention, however, is not to limit the invention to the particular embodiments described. On the contrary, the invention is intended to cover all modifications, equivalents, and alternatives falling within the scope of the invention as defined by the appended claims.
The outer walls of the heart 12 are lined with a tissue known as the epicardium 28. The inner walls of the heart are lined with a tissue known as the endocardium 30. The heart muscle, or myocardium 32, is sandwiched between the endocardium 30 and the epicardium 28. A tough outer pericardial sac 33 surrounds the heart 12.
The pacing system 10 includes a pulse generator 34 coupled to a myocardial lead 36. The pulse generator 34 is typically implanted in a pocket formed underneath the skin of the patient's chest or abdominal region. The lead 36 extends from the pulse generator 34 to the heart 12 and is implanted in the myocardium 32 near an apex 38 of the heart 12. The lead 36 delivers electrical signals from the pulse generator 34 to an electrode on the lead 36 to accomplish pacing of the heart 12 (not visible in
The lead 36 and anchor mechanism 44 may be implanted in the heart 12 via a delivery instrument and according to methods described in above-identified “Myocardial Lead Attachment System”. Briefly, the delivery instrument is used to pierce the epicardium 30 and draw anchor mechanism 44 and the tether 45 through the myocardium 32. As the delivery instrument traverses the myocardium 32, it creates a tract (not visible in
After the delivery instrument is removed, the lead 36 is threaded onto the tether 45 and advanced over the tether 45 into the heart 12. The tether 45 is tensioned and coupled to the lead 36 to secure the lead 36 in a stable position.
The lock arrangement can be any configuration that securely attaches the lead 36 to the tether 45. In the present embodiment, the lock housing 49 is a cavity 50 formed in the internal lumen 43 proximal to the distal tip 42 of the lead 36. A non-resilient internal ring 52 is positioned about the lumen 43 proximal to the cavity 50. The ring 52 has a diameter smaller than the size of the lock 48. While the distal tip 42 of the lead 36 is sufficiently resilient to expand and allow the lock 48 to enter the lead 36, the ring 52 does not deflect, and the lead 36 is prevented from advancing past the lock 48.
When the lead 102 has been properly positioned against the lock 118 such that the lock 118 is mated with in the lock housing 126, the tether 112 is placed under tension relative to the lead 102 by applying a tensile force to the portion of the tether 112 exiting through the through hole 140. The tensioned tether 112 is then fixed to the lead 102 at an attachment site near the through hole 140. In this manner, the myocardial lead 102 is fixed along the tether 112 between the lock 118 and the attachment site, which retains the lead 102 in a consistent position within the myocardium 32.
According to one embodiment, the tether 112 is fixed to the lead 102 by forming a knot 142 in the tensioned tether 112 just outside the through hole 140 (See
The lock structure 118 may take various shapes, and may be a separate member from the tether 112, for example a clip or other structure, fastened to the tether 112. In still other embodiments, the lock 118 and lock housing 126 may have other complementary mating shapes, which operate to inhibit motion of the lock 118 with respect to the lock housing 126.
The preceding embodiments generally describe fixation systems for fixing the distal end of the lead in position. According to other embodiments of the present invention, proximal fixation systems are provided for fixing the proximal end of the lead in a selected position.
According to one embodiment, as shown in
According to one embodiment, the tether 308 is formed of 0.0095 inch diameter polypropylene and a single knot 316 of the tether 308 is about 0.040 inches long by about 0.030 inches wide.
According to one embodiment, both a distal and a proximal attachment system are used to secure the lead to the tether. The combination of a proximal locking arrangement and a distal locking arrangement stabilize the lead within the heart 12 and reduce the likelihood of migrations of the lead from the implant site. Furthermore, the lead can be positioned in the heart 12 in a variety of configurations, including epicardial-epicardial, as is shown in the preceding figures, or epicardial-endocardial, intra-myocardial and pericardial-pericardial, as is described in above-identified application entitled “Myocardial Lead Attachment System.”
Various modifications and additions can be made to the exemplary embodiments discussed without departing from the scope of the present invention. Accordingly, the scope of the present invention is intended to embrace all such alternative, modifications, and variations as fall within the scope of the claims, together with all equivalents thereof.
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|Citing Patent||Filing date||Publication date||Applicant||Title|
|US20160030733 *||Jan 14, 2013||Feb 4, 2016||Peter Osypka||Myocardial heart pacemaker electrode|
|U.S. Classification||607/126, 607/130, 607/129|
|Cooperative Classification||A61N2001/0578, A61N1/0587|
|Mar 2, 2005||AS||Assignment|
Owner name: CARDIAC PACEMAKERS, INC., MINNESOTA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:COE, M. SEAN;HEIL, JR., RONALD W.;KELLEY, PETER T.;AND OTHERS;REEL/FRAME:015815/0087;SIGNING DATES FROM 20041021 TO 20041026
|Sep 15, 2009||CC||Certificate of correction|
|Aug 8, 2012||FPAY||Fee payment|
Year of fee payment: 4
|Aug 18, 2016||FPAY||Fee payment|
Year of fee payment: 8